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6418-38-8 Usage

Uses

Intermediates of Liquid Crystals

Check Digit Verification of cas no

The CAS Registry Mumber 6418-38-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,1 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6418-38:
(6*6)+(5*4)+(4*1)+(3*8)+(2*3)+(1*8)=98
98 % 10 = 8
So 6418-38-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H4F2O/c7-4-2-1-3-5(9)6(4)8/h1-3,9H

6418-38-8 Well-known Company Product Price

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  • Alfa Aesar

  • (A16971)  2,3-Difluorophenol, 98+%   

  • 6418-38-8

  • 1g

  • 247.0CNY

  • Detail
  • Alfa Aesar

  • (A16971)  2,3-Difluorophenol, 98+%   

  • 6418-38-8

  • 5g

  • 867.0CNY

  • Detail

6418-38-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-Difluorophenol

1.2 Other means of identification

Product number -
Other names 4-hydroxy-2,3-difluorobenzene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6418-38-8 SDS

6418-38-8Synthetic route

ortho-difluorobenzene
367-11-3

ortho-difluorobenzene

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

Conditions
ConditionsYield
Stage #1: ortho-difluorobenzene With n-butyllithium In tetrahydrofuran at -78℃; for 1h;
Stage #2: With Trimethyl borate In tetrahydrofuran for 16h;
Stage #3: With dihydrogen peroxide In tetrahydrofuran for 3h;
96.49%
Stage #1: ortho-difluorobenzene With n-butyllithium In tetrahydrofuran at -78℃; for 1h;
Stage #2: With Trimethyl borate In tetrahydrofuran for 16h;
Stage #3: With dihydrogen peroxide In tetrahydrofuran for 3h;
93.96%
With n-butyllithium; Triisopropyl borate; dihydrogen peroxide 1.) THF/hexane, -78 deg C, 2.5 h; 2.) THF/hexane, rt.; 3.) ether, 2.5 h, reflux; Yield given. Multistep reaction;
(2,3-difluorophenyl)boronic acid
121219-16-7

(2,3-difluorophenyl)boronic acid

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

Conditions
ConditionsYield
With dihydrogen peroxide In diethyl ether for 2.5h; Oxidation; Heating;100%
With 10-methylacridine-3(10H)-one; oxygen; N-ethyl-N,N-diisopropylamine In water at 20℃; for 20h; Irradiation; Green chemistry;98%
With dihydrogen peroxide In diethyl ether; water Reflux;94%
1-ethoxy-2,3-difluorobenzene

1-ethoxy-2,3-difluorobenzene

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

Conditions
ConditionsYield
With iron(III) chloride In diethyl ether at 30℃; for 5h; Temperature; Reagent/catalyst; Solvent;12.3 g
With boron trifluoride diethyl etherate In tetrahydrofuran at 50℃; for 10h;12.8 g
1,2-difluoro-3-n-propoxybenzene
124728-93-4

1,2-difluoro-3-n-propoxybenzene

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

Conditions
ConditionsYield
With iron(III) chloride In ethanol at 30℃; for 3h;10.6 g
2.3-difluoroanisole
134364-69-5

2.3-difluoroanisole

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

Conditions
ConditionsYield
With aluminum (III) chloride In methanol at 30℃; for 5h; Solvent;11.6 g
1,1,2-Trifluoro-7-oxabicyclo[2.2.1]hept-4-ene

1,1,2-Trifluoro-7-oxabicyclo[2.2.1]hept-4-ene

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

Conditions
ConditionsYield
With lithium diisopropyl amide In tetrahydrofuran at -70 - 20℃; for 3.5h; Elimination; Aromatization;25%
1,2,3-trifluorobenzene
1489-53-8

1,2,3-trifluorobenzene

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: sodium hydroxide / 20 h / 50 °C
2: aluminum (III) chloride / methanol / 5 h / 30 °C
View Scheme
Multi-step reaction with 2 steps
1: sodium hydroxide / 15 h / 50 °C
2: iron(III) chloride / diethyl ether / 5 h / 30 °C
View Scheme
C12H17BF2O2

C12H17BF2O2

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 100 percent / 10 percent aq. HCl / 1 h / 20 °C
2: 100 percent / 10 percent aq. H2O2 / diethyl ether / 2.5 h / Heating
View Scheme
C8H9BF2O2

C8H9BF2O2

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: hydrogenchloride; water / tetrahydrofuran
2: dihydrogen peroxide / diethyl ether; water / 1 h / Reflux
View Scheme
2,3-difluorobenzaldehyde
2646-91-5

2,3-difluorobenzaldehyde

A

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

B

2,3-difluorobenzoic acid
4519-39-5

2,3-difluorobenzoic acid

Conditions
ConditionsYield
With 4-hydroxyacetophenone monooxygenase from P. fluorescens ACB; oxygen; NADPH In phosphate buffer at 30℃; for 1h; pH=8.0; Enzyme kinetics; Baeyer-Villiger oxidation;
1,2,3-trifluorobenzene
1489-53-8

1,2,3-trifluorobenzene

A

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

B

3-fluorocatechol
363-52-0

3-fluorocatechol

Conditions
ConditionsYield
With dihydrogen peroxide In water pH=5; Kinetics; Oxidation; Photolysis; 254 nm;
1,2,3-trifluorobenzene
1489-53-8

1,2,3-trifluorobenzene

A

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

B

3-fluorocatechol
363-52-0

3-fluorocatechol

C

1,2,3-trihydroxy-4,5,6-trifluorobenzene

1,2,3-trihydroxy-4,5,6-trifluorobenzene

Conditions
ConditionsYield
With dihydrogen peroxide; oxygen In water pH=5; Kinetics; Quantum yield; Oxidation; Photolysis; 254 nm;
2,3-difluomuconate

2,3-difluomuconate

A

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

B

5-fluoroprotoanemonin

5-fluoroprotoanemonin

C

5-fluoromaleylacetate

5-fluoromaleylacetate

Conditions
ConditionsYield
With chloromuconate cycloisomerase Product distribution; Cyclization; Enzymatic reaction;
2,3-difluorophenol
6418-38-8

2,3-difluorophenol

methyl iodide
74-88-4

methyl iodide

2.3-difluoroanisole
134364-69-5

2.3-difluoroanisole

Conditions
ConditionsYield
With potassium carbonate In dimethyl sulfoxide at 20℃;100%
With potassium carbonate In acetone at 20 - 30℃; for 16h; Inert atmosphere;100%
With potassium carbonate In dimethyl sulfoxide at 20℃; for 0.5h;78%
2,3-difluorophenol
6418-38-8

2,3-difluorophenol

acetyl chloride
75-36-5

acetyl chloride

2,3-difluorophenyl acetate
851936-86-2

2,3-difluorophenyl acetate

Conditions
ConditionsYield
With pyridine In dichloromethane at 0 - 20℃; for 16h;100%
With pyridine In dichloromethane at 0 - 20℃; for 16h;100%
With pyridine In dichloromethane at 0 - 20℃; for 16h;100%
With pyridine In dichloromethane for 2h;99%
With pyridine In dichloromethane at 20℃; for 2h;
2,3-difluorophenol
6418-38-8

2,3-difluorophenol

ethyl iodide
75-03-6

ethyl iodide

1-ethoxy-2,3-difluorobenzene

1-ethoxy-2,3-difluorobenzene

Conditions
ConditionsYield
With potassium carbonate In acetone at 70℃; for 3h; Inert atmosphere;100%
With potassium carbonate In acetone at 70℃; for 5h;99.4%
2,3-difluorophenol
6418-38-8

2,3-difluorophenol

chloroacetyl chloride
79-04-9

chloroacetyl chloride

2,3-difluorophenyl-2-chloroacetate

2,3-difluorophenyl-2-chloroacetate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃;100%
2,3-difluorophenol
6418-38-8

2,3-difluorophenol

chloromethyl methyl ether
107-30-2

chloromethyl methyl ether

1,2-difluoro-3-(methoxymethoxy)benzene

1,2-difluoro-3-(methoxymethoxy)benzene

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0℃; for 2h;99.4%
With N-ethyl-N,N-diisopropylamine In dichloromethane at 0℃; for 2h;99.4%
With N-ethyl-N,N-diisopropylamine In dichloromethane at 25℃; for 2h;82%
2,3-difluorophenol
6418-38-8

2,3-difluorophenol

4-(2-chloroethyl)morpholine hydrochride
3647-69-6

4-(2-chloroethyl)morpholine hydrochride

4-(2-(2,3-difluorophenoxy)ethyl)morpholine

4-(2-(2,3-difluorophenoxy)ethyl)morpholine

Conditions
ConditionsYield
With tetra-(n-butyl)ammonium iodide; caesium carbonate In acetonitrile at 65℃; for 4h;99%
4-fluoro-2-methoxy-1-nitrobenzene
448-19-1

4-fluoro-2-methoxy-1-nitrobenzene

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

4-(2,3-difluoro-phenoxy)-2-methoxy-1-nitro-benzene

4-(2,3-difluoro-phenoxy)-2-methoxy-1-nitro-benzene

Conditions
ConditionsYield
With caesium carbonate In N,N-dimethyl-formamide at 120℃; for 3h;98%
1-Bromoheptane
629-04-9

1-Bromoheptane

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

2,3-difluoro-4-(heptyloxy)benzene
122265-84-3

2,3-difluoro-4-(heptyloxy)benzene

Conditions
ConditionsYield
With potassium carbonate In butanone Heating / reflux;97%
With potassium carbonate In ethyl acetate Heating;90%
With potassium carbonate In acetone for 48h; Alkylation; Heating;
With potassium hydroxide In ethanol
With sodium hydroxide In dimethyl sulfoxide
1-Bromononane
693-58-3

1-Bromononane

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

2,3-difluoro-4-(nonyloxy)benzene
122265-85-4

2,3-difluoro-4-(nonyloxy)benzene

Conditions
ConditionsYield
With potassium carbonate In ethyl acetate Heating;97%
With potassium carbonate In acetone for 48h; Alkylation; Heating;
With potassium hydroxide In ethanol
2,3-difluorophenol
6418-38-8

2,3-difluorophenol

tert-butyldimethylsilyl chloride
18162-48-6

tert-butyldimethylsilyl chloride

2,3-difluoro-(tert-butyldimethylsilyloxy)benzene
870646-82-5

2,3-difluoro-(tert-butyldimethylsilyloxy)benzene

Conditions
ConditionsYield
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 3h;97%
With dmap; triethylamine In dichloromethane at -15 - 0℃; Inert atmosphere;147.1 g
ethyl bromide
74-96-4

ethyl bromide

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

1-ethoxy-2,3-difluorobenzene

1-ethoxy-2,3-difluorobenzene

Conditions
ConditionsYield
With sodium hydroxide; tetrabutylammomium bromide In water at 80℃; for 6h; Inert atmosphere;97%
With tetramethlyammonium chloride; sodium hydroxide In water; N,N-dimethyl-formamide; toluene at 30℃; Reflux; Industrial scale;91.7%
1-bromo-hexane
111-25-1

1-bromo-hexane

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

1,2-difluoro-3-hexyloxybenzene
121219-19-0

1,2-difluoro-3-hexyloxybenzene

Conditions
ConditionsYield
With potassium carbonate In acetone for 43h; Heating;96%
With potassium carbonate In acetone for 48h; Alkylation; Heating;
trans-4-chloromethyl-1-pentylcyclohexane

trans-4-chloromethyl-1-pentylcyclohexane

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

2,3-difluoro-4-(trans-4-pentylcyclohexylmethoxy)benzene

2,3-difluoro-4-(trans-4-pentylcyclohexylmethoxy)benzene

Conditions
ConditionsYield
With potassium phosphate In N,N-dimethyl-formamide at 70℃; for 7h; Inert atmosphere;95.1%
2,3-difluorophenol
6418-38-8

2,3-difluorophenol

1-(benzyloxy)-2,3-difluorobenzene
144292-53-5

1-(benzyloxy)-2,3-difluorobenzene

Conditions
ConditionsYield
With potassium carbonate In water; N,N-dimethyl-formamide95.1%
triisopropylsilyl chloride
13154-24-0

triisopropylsilyl chloride

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

(2,3-difluorophenoxy)triisopropylsilane
749230-30-6

(2,3-difluorophenoxy)triisopropylsilane

Conditions
ConditionsYield
With 1H-imidazole at 20℃; for 18h;95%
With 1H-imidazole In N,N-dimethyl-formamide at 25℃; for 20h;94%
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 18h;
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 18h;
2,3-difluorophenol
6418-38-8

2,3-difluorophenol

tetra(n-butyl)ammonium hydrogensulfate
32503-27-8

tetra(n-butyl)ammonium hydrogensulfate

tetrabutylammonium 2,3‐difluorophenyl sulfate

tetrabutylammonium 2,3‐difluorophenyl sulfate

Conditions
ConditionsYield
Stage #1: 2,3-difluorophenol With chlorosulfonic acid; triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere;
Stage #2: With sodium hydroxide In dichloromethane; water
Stage #3: tetra(n-butyl)ammonium hydrogensulfate In dichloromethane; water
95%
1-bromo-octane
111-83-1

1-bromo-octane

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

2,3-difluoro-1-n-octyloxybenzene
121219-21-4

2,3-difluoro-1-n-octyloxybenzene

Conditions
ConditionsYield
With potassium carbonate In acetone for 12h; Heating;93%
With potassium carbonate In butanone for 12h; Inert atmosphere; Reflux;93%
With potassium carbonate In N,N-dimethyl-formamide for 6h; Heating;92%
1-Bromotetradecane
112-71-0

1-Bromotetradecane

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

1-tetradecyloxy-2,3-difluorobenzene

1-tetradecyloxy-2,3-difluorobenzene

Conditions
ConditionsYield
With potassium carbonate; potassium iodide In acetone for 48h; Reflux;93%
With potassium carbonate; potassium iodide In acetone for 48h; Reflux;93%
With potassium hydroxide In ethanol
2,3-difluorophenol
6418-38-8

2,3-difluorophenol

1-dodecylbromide
143-15-7

1-dodecylbromide

1,2-Difluoro-3-dodecyloxybenzene
122265-83-2

1,2-Difluoro-3-dodecyloxybenzene

Conditions
ConditionsYield
With potassium carbonate In ethyl acetate Heating;92%
With potassium carbonate In N,N-dimethyl-formamide for 6h; Heating;
With potassium hydroxide In ethanol
1-Bromopentane
110-53-2

1-Bromopentane

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

1,2-difluoro-3-pentyloxybenzene
156684-90-1

1,2-difluoro-3-pentyloxybenzene

Conditions
ConditionsYield
With potassium carbonate In acetone for 48h; Alkylation; Heating;92%
With potassium carbonate In butanone Heating;
2,3-difluorophenol
6418-38-8

2,3-difluorophenol

2-(2,3-Difluorophenoxy)-1-ethanol
313655-62-8

2-(2,3-Difluorophenoxy)-1-ethanol

Conditions
ConditionsYield
92%
2,3-difluorophenol
6418-38-8

2,3-difluorophenol

1-iodo-propane
107-08-4

1-iodo-propane

1,2-difluoro-3-n-propoxybenzene
124728-93-4

1,2-difluoro-3-n-propoxybenzene

Conditions
ConditionsYield
With sodium carbonate In ethanol; water92%
2,3-difluorophenol
6418-38-8

2,3-difluorophenol

2-Chloro-2-oxo-1,3,2-dioxaphospholane
6609-64-9

2-Chloro-2-oxo-1,3,2-dioxaphospholane

C8H7F2O4P

C8H7F2O4P

Conditions
ConditionsYield
In dichloromethane at 0 - 20℃; for 12h;92%
2,3-difluorophenol
6418-38-8

2,3-difluorophenol

2-chloro-1,3,2-dioxaphospholan
822-39-9

2-chloro-1,3,2-dioxaphospholan

2-(2,3-difluorophenoxy)-1,3,2-dioxaphospholane

2-(2,3-difluorophenoxy)-1,3,2-dioxaphospholane

Conditions
ConditionsYield
Stage #1: 2,3-difluorophenol In dichloromethane at 20℃; for 0.5h;
Stage #2: 2-chloro-1,3,2-dioxaphospholan In dichloromethane at 0 - 20℃; for 12h;
92%
2,3-difluorophenol
6418-38-8

2,3-difluorophenol

6-bromo-2,3-difluoro-phenol
186590-23-8

6-bromo-2,3-difluoro-phenol

Conditions
ConditionsYield
With bromine; tert-butylamine In dichloromethane; toluene at -78 - 20℃;91%
With bromine; tert-butylamine In dichloromethane; toluene at -78 - 20℃; for 5.5h;91%
With N-Bromosuccinimide; isopropylamine In dichloromethane at -30 - 20℃;80%
2,3-difluorophenol
6418-38-8

2,3-difluorophenol

tert-butyl 3-hydroxyazetidine-1-carboxylate
141699-55-0

tert-butyl 3-hydroxyazetidine-1-carboxylate

tert-butyl 3-(2,3-difluorophenoxy)azetidin-1-carboxylate

tert-butyl 3-(2,3-difluorophenoxy)azetidin-1-carboxylate

Conditions
ConditionsYield
With triphenylphosphine In tetrahydrofuran at 70℃; for 20h;91%
n-Butyl chloride
109-69-3

n-Butyl chloride

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

2,3-difluorophenyl butyl ether

2,3-difluorophenyl butyl ether

Conditions
ConditionsYield
With trimethylbenzylammonium bromide; potassium hydroxide In 5,5-dimethyl-1,3-cyclohexadiene; water; N,N-dimethyl-formamide at 30℃; Reflux; Industrial scale;90.8%
1-Chloropropane
540-54-5

1-Chloropropane

2,3-difluorophenol
6418-38-8

2,3-difluorophenol

1,2-difluoro-3-n-propoxybenzene
124728-93-4

1,2-difluoro-3-n-propoxybenzene

Conditions
ConditionsYield
With tetrabutylammomium bromide; potassium hydroxide In water; N,N-dimethyl-formamide; toluene at 30℃; Reflux; Industrial scale;90.6%

6418-38-8Relevant articles and documents

19F NMR study on the biodegradation of fluorophenols by various Rhodococcus species

Bondar, Vladimir S.,Boersma, Marelle G.,Golovlev, Eugene L.,Vervoort, Jacques,Van Berkel, Willem J.H.,Finkelstein, Zoya I.,Solyanikova, Inna P.,Golovleva, Ludmila A.,Rietjens, Ivonne M.C.M.

, p. 475 - 486 (1998)

Of all NMR observable isotopes 19F is the one perhaps most convenient for studies on biodegradation of environmental pollutants. THe reasons underlying this potential of 19F NMR are discussed are illustrated on the basis of a study on the biodegradation of fluorophenols by four Rhodococcus strains. The results indicate marked differences between the biodegradation pathways of fluorophenols among the various Rhodococcus species. This holds not only for the level and nature of the fluorinated biodegradation pathway intermediates that accumulate, but also for the regioselectivity of the initial hyroxylation step. Several of the Rhodococcus species contain a phenol hydroxylase that catalyses the oxidative defluorination of ortho- fluorinated di- and trifluorophenols. Furthermore it is illustrated how the 19F NMR technique can be used as a tool in the process of identification of an accumulated unknown metabolite, in this case most likely 5- fluoromaleylacetate. Altogether, the 19F NMR technique proved valid to obtain detailed information on the microbial biodegradation pathways of fluorinated organics, but also provide information on the specificity of enzymes generally considered unstable and, for this reason, not much studied so far.

INHIBITORS OF THE BCL6 BTB DOMAIN PROTEIN-PROTEIN INTERACTION AND USES THEREOF

-

Paragraph 00275, (2019/08/29)

The present application relates to compounds of Formula I (I) or pharmaceutically acceptable salts, solvates and/or prodrugs thereof, to compositions comprising these compounds or pharmaceutically acceptable salts, solvates and/or prodrugs thereof, and various uses in the treatment of diseases, disorders or conditions that are treatable by inhibiting interactions with BCL6 BTB, such as cancer.

A process for the preparation of 2, 3 - difluoro-phenol method (by machine translation)

-

Paragraph 0039; 0041; 0044; 0047, (2018/10/19)

The invention relates to a process for preparing 2, 3 - difluoro of phenol, to 1, 2, 3 - trifluorobenzene as raw materials, the solid super strong alkali catalytic alkoxylated and dealkylating reaction to prepare 2, 3 - difluoro phenol, synthesis route is short, simple process operation, without special equipment, yield up to 94.8% or more, and has excellent industrial prospect. (by machine translation)

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